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Stratum RS

FDA UDI

Class I (US FDA UDI)

by Medartis Inc.

Identity

Trade Name
Stratum RS FDA UDI
Generic Name
Orthopaedic intraoperative positioning pin, single-use FDA UDI
Device Name
Stratum Screw Driver Hex 2mm ST FDA UDI
Model / Reference
STRM-DRV-HEX-2MM FDA UDI
Description
Stratum Screw Driver Hex 2mm ST FDA UDI

Identifiers

Primary DI / UDI-DI
00817701028024 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic intraoperative positioning pin, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic intraoperative positioning pin, single-use

Stratum RS by Medartis Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic intraoperative positioning pin, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medartis Inc.

Sources (1)

  • FDA UDI 56abda07-3a7f-4b9b-beb4-ce1781e91131 33 fields · synced May 30, 2026